FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OSTEO CERCLAGE WIRE

K Number: K914374 · Decision Dec 30, 1991
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
9
Review Days
90

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Basic Information

Device Name
OSTEO CERCLAGE WIRE
K Number
K914374
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Osteo AG
Date Received
October 1, 1991
Decision Date
December 30, 1991
Product Code
JDQ
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JDQ Cerclage, Fixation

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Other Clearances by Osteo AG

K Number Device Name
K933340 OSTEO INTERLOCKING-COMPRESSION NAIL
K922196 OSTEO TIBIA NAIL
K922195 OSTEO FEMORAL NAIL
K922193 OSTEO KIRSCHNER WIRE
K922194 OSTEO STEINMANN PIN
K920149 OSTEO EX-FI-RE
K920037 OSTEO COMPRESSION HIP SCREW
K913559 OSTEO COMPLETE PNEUMATIC DRILL-OSCILAIR